IE60271B1 - "Thiol/ene compositions" - Google Patents
"Thiol/ene compositions"Info
- Publication number
- IE60271B1 IE60271B1 IE3286A IE3286A IE60271B1 IE 60271 B1 IE60271 B1 IE 60271B1 IE 3286 A IE3286 A IE 3286A IE 3286 A IE3286 A IE 3286A IE 60271 B1 IE60271 B1 IE 60271B1
- Authority
- IE
- Ireland
- Prior art keywords
- radical
- free
- alkenyl
- group
- groups
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 80
- 125000003396 thiol group Chemical class [H]S* 0.000 title claims description 5
- 150000001875 compounds Chemical class 0.000 claims abstract description 26
- -1 isopropenyl hydrogen Chemical class 0.000 claims abstract description 25
- 125000003342 alkenyl group Chemical group 0.000 claims abstract description 22
- 125000000392 cycloalkenyl group Chemical group 0.000 claims abstract description 17
- 239000004215 Carbon black (E152) Substances 0.000 claims abstract description 16
- 229930195733 hydrocarbon Natural products 0.000 claims abstract description 16
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 14
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims abstract description 14
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 13
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims abstract description 13
- 239000007795 chemical reaction product Substances 0.000 claims abstract description 11
- 229920002554 vinyl polymer Polymers 0.000 claims abstract description 10
- STMDPCBYJCIZOD-UHFFFAOYSA-N 2-(2,4-dinitroanilino)-4-methylpentanoic acid Chemical compound CC(C)CC(C(O)=O)NC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O STMDPCBYJCIZOD-UHFFFAOYSA-N 0.000 claims abstract description 9
- 125000006017 1-propenyl group Chemical group 0.000 claims abstract description 8
- 125000000555 isopropenyl group Chemical group [H]\C([H])=C(\*)C([H])([H])[H] 0.000 claims abstract description 8
- 239000000178 monomer Substances 0.000 claims abstract description 8
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 7
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 claims abstract description 6
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 claims abstract description 5
- 239000004593 Epoxy Substances 0.000 claims abstract description 4
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 4
- 239000004205 dimethyl polysiloxane Substances 0.000 claims abstract description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 4
- 125000004122 cyclic group Chemical group 0.000 claims abstract description 3
- 239000001257 hydrogen Substances 0.000 claims abstract description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract 2
- ZWAJLVLEBYIOTI-UHFFFAOYSA-N cyclohexene oxide Chemical group C1CCCC2OC21 ZWAJLVLEBYIOTI-UHFFFAOYSA-N 0.000 claims abstract 2
- 238000000576 coating method Methods 0.000 claims description 18
- 150000002148 esters Chemical class 0.000 claims description 16
- 150000003254 radicals Chemical class 0.000 claims description 16
- 239000011248 coating agent Substances 0.000 claims description 12
- 238000001723 curing Methods 0.000 claims description 8
- 150000008064 anhydrides Chemical class 0.000 claims description 6
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims description 6
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 5
- 239000002253 acid Substances 0.000 claims description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
- 150000001805 chlorine compounds Chemical class 0.000 claims description 4
- 235000013870 dimethyl polysiloxane Nutrition 0.000 claims description 4
- 239000012948 isocyanate Substances 0.000 claims description 4
- 150000002513 isocyanates Chemical class 0.000 claims description 4
- 229920000647 polyepoxide Polymers 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 3
- 150000001299 aldehydes Chemical class 0.000 claims description 2
- 125000005011 alkyl ether group Chemical group 0.000 claims description 2
- 125000000746 allylic group Chemical group 0.000 claims description 2
- 150000001735 carboxylic acids Chemical class 0.000 claims description 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 2
- 238000000016 photochemical curing Methods 0.000 claims description 2
- 239000000758 substrate Substances 0.000 claims 3
- 229940125773 compound 10 Drugs 0.000 claims 1
- 230000001678 irradiating effect Effects 0.000 claims 1
- ZLVXBBHTMQJRSX-VMGNSXQWSA-N jdtic Chemical compound C1([C@]2(C)CCN(C[C@@H]2C)C[C@H](C(C)C)NC(=O)[C@@H]2NCC3=CC(O)=CC=C3C2)=CC=CC(O)=C1 ZLVXBBHTMQJRSX-VMGNSXQWSA-N 0.000 claims 1
- 150000003573 thiols Chemical class 0.000 abstract description 15
- 125000006238 prop-1-en-1-yl group Chemical group [H]\C(*)=C(/[H])C([H])([H])[H] 0.000 abstract description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 16
- 229920005989 resin Polymers 0.000 description 16
- 239000011347 resin Substances 0.000 description 16
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 12
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 11
- 239000000463 material Substances 0.000 description 10
- BJIOGJUNALELMI-ONEGZZNKSA-N Isoeugenol Natural products COC1=CC(\C=C\C)=CC=C1O BJIOGJUNALELMI-ONEGZZNKSA-N 0.000 description 9
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- BJIOGJUNALELMI-ARJAWSKDSA-N cis-isoeugenol Chemical compound COC1=CC(\C=C/C)=CC=C1O BJIOGJUNALELMI-ARJAWSKDSA-N 0.000 description 9
- 238000002156 mixing Methods 0.000 description 9
- 239000002904 solvent Substances 0.000 description 9
- BJIOGJUNALELMI-UHFFFAOYSA-N trans-isoeugenol Natural products COC1=CC(C=CC)=CC=C1O BJIOGJUNALELMI-UHFFFAOYSA-N 0.000 description 9
- 229920001429 chelating resin Polymers 0.000 description 8
- 239000007788 liquid Substances 0.000 description 8
- KWVGIHKZDCUPEU-UHFFFAOYSA-N 2,2-dimethoxy-2-phenylacetophenone Chemical compound C=1C=CC=CC=1C(OC)(OC)C(=O)C1=CC=CC=C1 KWVGIHKZDCUPEU-UHFFFAOYSA-N 0.000 description 7
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 7
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 6
- 229910000027 potassium carbonate Inorganic materials 0.000 description 6
- 239000007787 solid Substances 0.000 description 6
- BHELZAPQIKSEDF-UHFFFAOYSA-N allyl bromide Chemical compound BrCC=C BHELZAPQIKSEDF-UHFFFAOYSA-N 0.000 description 5
- 238000004458 analytical method Methods 0.000 description 5
- 238000010992 reflux Methods 0.000 description 5
- 239000000047 product Substances 0.000 description 4
- 238000004611 spectroscopical analysis Methods 0.000 description 4
- 239000000725 suspension Substances 0.000 description 4
- ZSZUAWYMYCAJNX-UHFFFAOYSA-N 1-ethenyl-4-prop-2-enoxybenzene Chemical compound C=CCOC1=CC=C(C=C)C=C1 ZSZUAWYMYCAJNX-UHFFFAOYSA-N 0.000 description 3
- 101150041968 CDC13 gene Proteins 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 3
- 229910052753 mercury Inorganic materials 0.000 description 3
- 239000003208 petroleum Substances 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- 239000012258 stirred mixture Substances 0.000 description 3
- JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 3
- BLAHXQHYMANQBP-UHFFFAOYSA-N 1-(4-prop-2-enoxyphenyl)ethanone Chemical compound CC(=O)C1=CC=C(OCC=C)C=C1 BLAHXQHYMANQBP-UHFFFAOYSA-N 0.000 description 2
- PIZHFBODNLEQBL-UHFFFAOYSA-N 2,2-diethoxy-1-phenylethanone Chemical compound CCOC(OCC)C(=O)C1=CC=CC=C1 PIZHFBODNLEQBL-UHFFFAOYSA-N 0.000 description 2
- LHJZSWVADJCBNI-UHFFFAOYSA-N 2-methoxy-5-prop-1-enylphenol Chemical compound COC1=CC=C(C=CC)C=C1O LHJZSWVADJCBNI-UHFFFAOYSA-N 0.000 description 2
- TXFPEBPIARQUIG-UHFFFAOYSA-N 4'-hydroxyacetophenone Chemical compound CC(=O)C1=CC=C(O)C=C1 TXFPEBPIARQUIG-UHFFFAOYSA-N 0.000 description 2
- RGHHSNMVTDWUBI-UHFFFAOYSA-N 4-hydroxybenzaldehyde Chemical compound OC1=CC=C(C=O)C=C1 RGHHSNMVTDWUBI-UHFFFAOYSA-N 0.000 description 2
- TYNJQOJWNMZQFZ-UHFFFAOYSA-N 4-prop-2-enoxybenzaldehyde Chemical compound C=CCOC1=CC=C(C=O)C=C1 TYNJQOJWNMZQFZ-UHFFFAOYSA-N 0.000 description 2
- YXALYBMHAYZKAP-UHFFFAOYSA-N 7-oxabicyclo[4.1.0]heptan-4-ylmethyl 7-oxabicyclo[4.1.0]heptane-4-carboxylate Chemical compound C1CC2OC2CC1C(=O)OCC1CC2OC2CC1 YXALYBMHAYZKAP-UHFFFAOYSA-N 0.000 description 2
- HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- NIQCNGHVCWTJSM-UHFFFAOYSA-N Dimethyl phthalate Chemical compound COC(=O)C1=CC=CC=C1C(=O)OC NIQCNGHVCWTJSM-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000007859 condensation product Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 150000002118 epoxides Chemical class 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- JVTZFYYHCGSXJV-UHFFFAOYSA-N isovanillin Chemical compound COC1=CC=C(C=O)C=C1O JVTZFYYHCGSXJV-UHFFFAOYSA-N 0.000 description 2
- LSEFCHWGJNHZNT-UHFFFAOYSA-M methyl(triphenyl)phosphanium;bromide Chemical compound [Br-].C=1C=CC=CC=1[P+](C=1C=CC=CC=1)(C)C1=CC=CC=C1 LSEFCHWGJNHZNT-UHFFFAOYSA-M 0.000 description 2
- GKTNLYAAZKKMTQ-UHFFFAOYSA-N n-[bis(dimethylamino)phosphinimyl]-n-methylmethanamine Chemical class CN(C)P(=N)(N(C)C)N(C)C GKTNLYAAZKKMTQ-UHFFFAOYSA-N 0.000 description 2
- 229920006295 polythiol Polymers 0.000 description 2
- 239000000523 sample Substances 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000004809 thin layer chromatography Methods 0.000 description 2
- UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 1
- ULTHEAFYOOPTTB-UHFFFAOYSA-N 1,4-dibromobutane Chemical compound BrCCCCBr ULTHEAFYOOPTTB-UHFFFAOYSA-N 0.000 description 1
- VESSUVYGYNWKQE-UHFFFAOYSA-N 2-(3-phenylprop-2-enoxy)ethanol Chemical compound OCCOCC=CC1=CC=CC=C1 VESSUVYGYNWKQE-UHFFFAOYSA-N 0.000 description 1
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
- PMNLUUOXGOOLSP-UHFFFAOYSA-M 2-sulfanylpropanoate Chemical compound CC(S)C([O-])=O PMNLUUOXGOOLSP-UHFFFAOYSA-M 0.000 description 1
- DGWCHURQYFMBFC-UHFFFAOYSA-N 3-methoxy-4-prop-2-enoxybenzaldehyde Chemical compound COC1=CC(C=O)=CC=C1OCC=C DGWCHURQYFMBFC-UHFFFAOYSA-N 0.000 description 1
- 229940073735 4-hydroxy acetophenone Drugs 0.000 description 1
- WUDYMKBALKOCCE-UHFFFAOYSA-N 4-methoxy-3-prop-2-enoxybenzaldehyde Chemical compound COC1=CC=C(C=O)C=C1OCC=C WUDYMKBALKOCCE-UHFFFAOYSA-N 0.000 description 1
- JAGRUUPXPPLSRX-UHFFFAOYSA-N 4-prop-1-en-2-ylphenol Chemical compound CC(=C)C1=CC=C(O)C=C1 JAGRUUPXPPLSRX-UHFFFAOYSA-N 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229940123457 Free radical scavenger Drugs 0.000 description 1
- OWYWGLHRNBIFJP-UHFFFAOYSA-N Ipazine Chemical compound CCN(CC)C1=NC(Cl)=NC(NC(C)C)=N1 OWYWGLHRNBIFJP-UHFFFAOYSA-N 0.000 description 1
- 229930192627 Naphthoquinone Natural products 0.000 description 1
- 125000004036 acetal group Chemical group 0.000 description 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
- 150000001241 acetals Chemical class 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000002318 adhesion promoter Substances 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- 150000004054 benzoquinones Chemical class 0.000 description 1
- 235000010354 butylated hydroxytoluene Nutrition 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000010538 cationic polymerization reaction Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229930003836 cresol Natural products 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- WMPOZLHMGVKUEJ-UHFFFAOYSA-N decanedioyl dichloride Chemical compound ClC(=O)CCCCCCCCC(Cl)=O WMPOZLHMGVKUEJ-UHFFFAOYSA-N 0.000 description 1
- FBSAITBEAPNWJG-UHFFFAOYSA-N dimethyl phthalate Natural products CC(=O)OC1=CC=CC=C1OC(C)=O FBSAITBEAPNWJG-UHFFFAOYSA-N 0.000 description 1
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 description 1
- 229960001826 dimethylphthalate Drugs 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 229940093499 ethyl acetate Drugs 0.000 description 1
- 235000019439 ethyl acetate Nutrition 0.000 description 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 1
- 238000001030 gas--liquid chromatography Methods 0.000 description 1
- 238000005227 gel permeation chromatography Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000000687 hydroquinonyl group Chemical class C1(O)=C(C=C(O)C=C1)* 0.000 description 1
- 238000002329 infrared spectrum Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 239000013067 intermediate product Substances 0.000 description 1
- HLJDOURGTRAFHE-UHFFFAOYSA-N isocyanic acid;3,5,5-trimethylcyclohex-2-en-1-one Chemical compound N=C=O.N=C=O.CC1=CC(=O)CC(C)(C)C1 HLJDOURGTRAFHE-UHFFFAOYSA-N 0.000 description 1
- KCWDJXPPZHMEIK-UHFFFAOYSA-N isocyanic acid;toluene Chemical compound N=C=O.N=C=O.CC1=CC=CC=C1 KCWDJXPPZHMEIK-UHFFFAOYSA-N 0.000 description 1
- 238000001819 mass spectrum Methods 0.000 description 1
- 150000002791 naphthoquinones Chemical class 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000003504 photosensitizing agent Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 238000004382 potting Methods 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 238000000425 proton nuclear magnetic resonance spectrum Methods 0.000 description 1
- 239000002516 radical scavenger Substances 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- ODZPKZBBUMBTMG-UHFFFAOYSA-N sodium amide Chemical compound [NH2-].[Na+] ODZPKZBBUMBTMG-UHFFFAOYSA-N 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- LXEJRKJRKIFVNY-UHFFFAOYSA-N terephthaloyl chloride Chemical compound ClC(=O)C1=CC=C(C(Cl)=O)C=C1 LXEJRKJRKIFVNY-UHFFFAOYSA-N 0.000 description 1
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 description 1
- JRMUNVKIHCOMHV-UHFFFAOYSA-M tetrabutylammonium bromide Chemical compound [Br-].CCCC[N+](CCCC)(CCCC)CCCC JRMUNVKIHCOMHV-UHFFFAOYSA-M 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 239000012745 toughening agent Substances 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- MWOOGOJBHIARFG-UHFFFAOYSA-N vanillin Chemical compound COC1=CC(C=O)=CC=C1O MWOOGOJBHIARFG-UHFFFAOYSA-N 0.000 description 1
- FGQOOHJZONJGDT-UHFFFAOYSA-N vanillin Natural products COC1=CC(O)=CC(C=O)=C1 FGQOOHJZONJGDT-UHFFFAOYSA-N 0.000 description 1
- 235000012141 vanillin Nutrition 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/38—Polysiloxanes modified by chemical after-treatment
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/20—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring
- C07C43/23—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring containing hydroxy or O-metal groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F12/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring
- C08F12/34—Monomers containing two or more unsaturated aliphatic radicals
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Abstract
Curable thiol/ene compositions comprise: 1) a multifunctional styryloxy monomer having one or more of the following structures wherein R1, R2 and R3 are selected from vinyl (-CH=CH2), 1-propenyl(-CH=CH-CH3), isopropenyl hydrogen, lower alkyl or alkoxy, provided that at least one of R', R2 and R3 must be vinyl, 1-propenyl or isopropenyl; n is an integer ≥ 1; if n = 1, then R4 is a monovalent hydrocarbon radical containing one free-radically copolymerisable alkenyl or cycloalkenyl group, if n ≥2, R4 is a multivalent hydrocarbon radical which mav contain a maximum of one free-radicallv copolymerisable alkenyl or cycloalkenyl group; R5 is a divalent hydrocarbon radical; or a carbon atom which is part of a cyclic group in the radical G; or a radical of formula where R7 is a divalent hydrocarbon radical; if n = 1, G is a monovalent organic or inorganic radical, free of phenolic hydroxyl groups or other groups which substantially interfere with radical polymerisation, containing one free-radically copolymerisable alkenyl or cycloalkenyl group; if n ≥2, G is a multivalent organic or inorganic radical, free of phenolic hydroxyl groups or other groups which substantially interfere with radical polymerisation, which may contain a maximum of one free-radically copolymerisable alkenyl or cycloalkenyl group; R5 is a lower alkyl or cycloakyl group; or if n = 1, R5 may also be an alkenyl, or cycloalkenyl group, provided that G does not contain an alkenyl or cycloalkenyl group. 2) a multifunctional thiol. 3) a free-radical curing rate accelerator. Novel styryloxy compounds are described which are reaction products of a compound of the formula:where R' is vinyl, 1-propenyl or isopropenyl; R2 and R3 are H, lower alkyl or alkoxy; and R6 is alkyl, with an epoxy functional compound selected from the group consisting of: a) triglycidylether isocyanurate, b) allyl glycidyl ether, c) compounds having plural epoxy cyclohexane groups, and d) a multifunctional epoxidised polydimethylsiloxane which is the reaction product of allyl glycidyl ether with a dimethylsiloxane having 2 or more SiH groups.
Description
Thiol/ene Compositions This invention relates to curable thiol/ene compositions wherein the -ene component is a multifunctional styryloxy monomer.
Numerous proposals have been made for curable compositions 5 based on thiol/ene polymer systemst the essential components of which are a multifunctional alkene and a multifunctional thiol. Representative groups of thiol/ene polymers are described in US Patent 3 661 744 Kehr et al assigned to W.R. Grace & Co; and US Patent 4 008 341 Kehr, also assigned to W.R. Grace & Co; and US Patent 4 119 617 Hanyuda et al assigned to Showa Highpolvmer Co. Ltd.
US Patent 4 308 367 Green et al assigned to Ciba-Geigv Corporation discloses polymerisable compositions of the thiol/ ene type in which the -ene component is a compound containing in the same molecule at least one phenolic hydroxyl group and at least two groups chosen from allyls methallyl and 1-propenyl groups. However,, the phenolic hydroxyl group., being a freeradical scavenger, tends to decelerate the polymerisation reaction.
US Patent 4 145 479 Adams et al assigned to Armstrong Cork Company discloses a curable composition comprising at least one unsaturated polyaryloxyphosphazene, at least one aryloxy cyclotriphosphazene and a thiol crosslinking agent. Among the terminal groups suggested for the unsaturated phosphazene -2components are various styryloxy groups. However these compounds must have the phosphazene backbone structure,, which is linked to the oxygen of the styryloxy terminal groups by a P~0~ linkage, and the compounds are therefore distinct from those used in the present invention.
US Patent 4 543 397 Woods et al assigned to Loctite (Ireland) Limited discloses polyfunctional cationicallv polymerizable styryloxy compounds of the formula or wherein Rl and R^ are H, or one of R'- and R^ are H and the other is methyl; R3 and R^ are H9 lower alkyl, or alkoxy/ if r2 is not methyl; R^ is a divalent hydrocarbon radical; G is any multivalent organic or inorganic radical free of amino, aliphatic hydroxyl, aliphatic thiol or other groups which interfere with cationic polymerization; and n is an integer of two or more. -3The present invention provides novel curable compositions comprising 1) a multifunctional styryloxy monomer having one or more of the following structures OR wherein: R% R2 and R3 are selected from vinyl («CH=CH2)» 1-propenyl(-CH=CH-CH3), isopropenyl (OCH2), hydrogen, CH3 alkyl or alkoxy, provided that at least one of R^, R^ and R3 must be vinyl, 1-propenyl or isopropenyl; n is an integer'll; if n - 1. then R^ is a monovalent hydrocarbon radical containing one free-radically copolymerisable alkenyl or cycloalkenyl group. -4if n^2, R4 is a multivalent hydrocarbon radical which may contain a maximum of one free-radically copolymerisable alkenyl or cycloalkenyl group; r5 is a divalent hydrocarbon radical; or a carbon atom which is part of a cyclic group in the radical G; or a radical of γ II formula ~R'~C-O- where R' is a divalent hydrocarbon radical; if n s 18 G is a monovalent organic or inorganic radical, free of phenolic hydroxyT groups or other groups which substantially interfere with radical polymerisation, containing one free-radically copolymerisable alkenyl or cycloalkenyl group; if n ^2, G is a multivalent organic or inorganic radical, free of phenolic hydroxyl groups or other groups which substantially interfere with radical polymerisation, which may contain a maximum of one free-radically copolymerisable alkenyl or cycloalkenyl group; R5 is aC^-C^Q alkyl or cycloalkyl group; or if n = 1, R6 may also be an alkenyl or cycloalkenyl group, provided that G does not contain an alkenyl or cycloalkenyl group. 2) a multifunctional thiol. 3) a free-radical curing rate accelerator.
In the preferred embodiments C^-C^ alkyl is alkyl.
The mole ratio of styryloxy/thiol groups is suitably from 0.2/1 to 5/1, preferably 0.75/1 to 1.5/1. 9' -5R& way suitably be an alkenyl group e.g. an alJy_.li£L group.
When n - ls G may suitably be a substituted or unsubstituted monovalent hydrocarbon radical which may be straight or branched chain and which contains one free-radically copolymerisable alkenyl group, for example an allylic group or an allyl alkyl ether group, optionally substituted with a hydroxy group When n&2, G may suitably be a) a polyorganosiloxane backbone, optionally substituted with styryloxy groups of the kind defined within the square brackets above, b) an n-valent hydrocarbon radical, straight or branched chain. c) a urethane group d) an ester group e) an isocyanurate group f) an acetal group.
The invention also provides novel multifunctional styryloxy monomers including reaction products of a compound of the formula: OH where R~ is vinyl, l-propenyl or isopropenyl; R2 and R^ are H,C^-C^g alkyl or alkoxy; and R6 is alkyl, with an epoxy functional compound selected from: 6a) triglycidylether isocyanurate, b) allyl glycidyl ether, c) compounds having plural epo^y cyclohexane groups, and d) a multifunctional epoxidised polydimethylsiloxane which is the reaction product of allyl glycidyl ether with a di methyl siloxane having 2 or more SiH groups.
The multifunctional epoxidised polydimethyl siloxanes d) are generally of the formula wherein n is zero or an integer, preferably less than 50, particularly less than 20s for example 5, and m is an integer greater than about 10 and preferably less than 500, particularly less than 100, for example 30.
Preferred novel compounds are selected from the group consisting of: CH3—C=CH2 -oa~ ch=chch3Js The novel compounds are useful in the Thiol/ene compositions of the invention.
In addition to the compounds described in the Examples below, other suitable styryloxy monomers include the following: 1. Reaction products of hydroxyl containing styryloxy compounds with: a) Polyfunctional isocyanates. e.g. the urethane formed by reacting 2 equivalents of 4~(2-hydroxyethoxy)-3~methoxyprop-l-enylbenzene with 1 equivalent of di phenyl methane di isocyanate. b) Polyfunctional carboxylic acids or acid chlorides. e.g. the ester formed by reacting 2 equivalents of 4-([220 hydroxy-3(oxyprop-2-enyl)-propoxy]-prop-l-enylbenzene with equivalent of sebacoyl chloride. c) Di anhydrides. e.g. the ester formed by reacting 2 equivalents of 4-(2-7hydroxyethoxy)prop-l-enylbenzene with 1 equivalent of pyromellitic di anhydride. d) Aldehydes. e.g. the acetal formed by reacting 2 equivalents of 4-(25 hydroxyethoxy)prop-l-enylbenzene with one equivalent of acrolein. e) Polyepoxides. e.g. the styryloxy substituted Νονοίac resin formed by reacting 2.7 equivalents of 4-(2-hydroxyethoxy)prop-l10 enylbenzene with 1 equivalent of epoxy cresol Νονοίac Resin ECM 1235 (supplied by Ciba Geigy Corp.). f) Polyfunctional esters. e.g. the ester formed by reacting 2 equivalents of 4-(2hydroxyethoxy)prop-l-enylbenzene with one equivalent of dimethyl phthalate. 2. Reaction products of 3-hydroxy-4-alkoxystyrenes with a) Polyfunctional isocyanates. e.g. the urethane formed by reacting 2 equivalents of 2~methoxy-5-prop-l-enylphenol with 1 equivalent of isophorone di isocyanate. b) Di anhydrides. e.g. the ester formed by reacting 2 equivalents of 2methoxy-5-prop-l-enylphenol with 1 equivalent of 3,3',4,4'-benzophenone-tetracarboxylic di anhydride. c) Polyepoxides. e.g. the isocyanurate formed by reacting 3 equivalents of 2-methoxy-5-prop-l-enylphenol with 1 equivalent of triglycidyl ether isocyanurate. d) Multifunctional acid chlorides. e.g. the ester formed by reacting 2 equivalents of 2-methoxy-5-prop-l-enylphenol with 1 equivalent of terephthaloyl chloride. -8The multifunctional thiol may be chosen from compounds having 2 or more mercapto groups (-SH) per molecule. Suitable polythiols are described in US Patents 3 661 744, 4 008 341 and 4 119 617 mentioned above. The polythiol component suitably has a molecular weight in the range from about 50 to about 20,000 and is of the general formula Rn-(SH)n where R is a polyvalent organic moiety free from reactive carbon-to~carbon unsaturation and n is at least two.
The free radical curing rate accelerator may be of any of the known types of accelerator or polymerisation initiator which activate the composition photochemically, thermally or by chemical (Redox) action. Suitable photocuring rate accelerators are described in US Patent 3 661 744, particularly the aldyhyde and ketone carbonyl compounds having at least one aromatic nucleus attached directly to the ~C~ oroup. 0« Examples include benzophenone, acetophenone^ 2,2-dimethoxy~2~phenylacetophenone and derivatives thereof.
The rate accelerator may suitably' be present over the range 0.05-10% by weight of the total weight of the composition.
Optionally the composition may contain an organic solvent (e-g. ethylacetate or 1,1,1-trichloroethane) and a free radical stabiliser or inhibitor to prevent premature onset of curing (e.g. hydroquinones, benzoquinones, naphthoquinones, phenanthraquinones and substituted compounds of any of the foregoing, or phenols such as 2,6-di-tert-butyl-4-methyl phenol).
Other optional ingredients of the composition include coinitiators or photosensitizers, thickeners, pigments, dyes, toughening agents, antioxidants, acids (e.g. phosphorous acid). -9wetting agents, flow control agents and adhesion promoters, all of which are of types known in the prior art.
The present invention provides novel thiol/ene compositions which are capable of more rapid curing than commercially available thiol/ene systems and which have good thermal resistance. They can be used for numerous applications which are known for thiol/ene compositions, such as coatings, potting compositions and sealing and gasketting materials.
The invention is illustrated in the following examples: -10Example 1 A mixture of isoeugenol (24.6g), 3,4-epoxycyclohexylmethyl-3,4-epoxycyclohexane carboxylate (18.75g) (available under the trade name ERL-4221 from Union Carbide) and potassium hydroxide (0.09g) was heated at 100°C for 71 hours. After this time, thin layer chromatography (t.l.c.) indicated that the isoeugenol had been almost consumed. On cooling, a yellow solid was obtained. T.l.c. analysis of this material indicated the presence of many compounds and a mass spectrum showed the major component to be the difunctional styryloxy monomer (M+ at 580.4 = 12% CC^H^^Og]; (M-164)+ at 416.2 = 3% ί624Η320θ]; M/e = 164.1 [C^H^O?]) exemplified by the formula: along with material isomeric to this structure. Gel permeation chromatography (G.P.C.) showed that 60% of the resin corresponded to the difunctional styryloxy resin, 25% to higher molecular weight analogues and polymer and 15% to lower molecular weight compounds including minor amounts of the starting phenol.
Example 2 An ultra-violet (UV) light sensitive composition was prepared by heating to 80°C a mixture of 1.45g of the resin obtained in Example 1, 1.11q of pentaerythrital tetrakis mercaptopropionate (mercaptate Q-43 ester supplied by Cincinnati Milacron Chemicals) and 2,2-dimethoxy-2-phenylacetophenone (0.08g) until a homogeneous blend was obtained. A 100 micron thick coating of the blend was then prepared on a standard 1 x 4 microscope glass slide and the coating exposed to ultraviolet light, from a medium pressure mecury arc lamp operating at 200 W/inch (Porta-Cure 1UU0, American Ultraviolet Co.). -11After 5 seconds exposure, the coating had cured to a dry film which was found to be insoluble in acetone. The light intensity at the curing surface was measured using an International Light Co. light meter (model IL-443) with 365 nm probe and found to be 60mW/cnA Example 3.
Isoeugenol (16.47g)s allyl glycidyl ether (11.42g) and Amberlyst A-21 (2,02g) resin were heated together at 105°C for 8 hours. After this time, t.l.c. analysis indicated that most of the starting isoeugenol had been consumed. The Amberlyst resin was separated from the reaction mixture and the remaining brown coloured liquid was analysed by G.P.C. The chromoatogram showed only one peak corresponding to a higher molecular weight product than either of the starting compounds. This compound is believed to be the simple condensation product of the phenol and the epoxide and has the structure: Amberlyst A-21 is a commercially available weakly basic anion 20 exchange resin whose functional structures are dimethyl amino groups. Amberlyst is a Trade Mark of Rohm & Haas Company.
Example 4 U.V. sensitive compositions were prepared by blending the following materials together (all parts by weight): Composition A Composition B Resin of Example 3 Mercaptate Q 43 2p2-dimethoxy-2-phenyl acetophenone 51.3 45.0 3.7 66.8 29.3 3.9 Ί2" Coatings were prepared as described in Example 2. After 20 secs, exposure (UV conditions as Example 2), Composition A had cured to a tack-free film with good adhesion to the glass surface. Approximately 60 secs, exposure was required to cure Composition B which was softer than Composition A.
Example 5 4-isopropenylphenol (8.9g) [prepared by the method described by J. Kahovec et al, Collection Czechoslov. Chem. Commun., Vol. 36, page 1986. (1970)], allylglycidyl ether (7.6g) and Amberlyst A-21 resin (1.0g) were heated together at 115°C for 6.5 hours. After this time, t.l.c. analysis indicated that the starting phenol had been almost consumed. Removal of the Amberlyst resin gave a brown coloured liquid believed to be the condensation product of the starting phenol and epoxide, represented by the formula: OH OCH2CHCH2—och2ch=ch2 CH3—C—CH2 Example 6 UV sensitive compositions were prepared by blending the following materials together (wt. in grams): Composition C Composition D Reaction product of Example 5 Mercaptate Ester, Q43 2,2-dimethoxy-2-phenyl acetophenone 6.2 6,1 0.5 6.2 3.0 0.4 Coatings of these compositions were After 50 secs, exposure to UV light cured tack free films were obtained prepared as described in Example 2. (conditions as described in Example 2), Composition D was harder than Composition C. -13Example 7 12.5g of a heptafunctional epoxidised polydimethylsiloxane of approximate molecular weight 3.380 (prepared by a hydrosi1ation reaction of one equivalent of the corresponding heptafunctional hydro siloxane and seven equivalents of allyl glycidyl ether in the presence of a platinum catalyst), 2.22g of isoeugenol and 1.38 grams of Amberlyst Resin A-21 were heated together at 110°C for 17 hours. After this time, t.l.c. analysis indicated that all of the isoeugenol was consumed. The infra red (I.R.) spectrum of the reaction mixture showed a peak at 3480cm due to the presence of an hydroxyl group. The Amberlyst resin was separated from the reaction mixture to yield a product predominately of the formula: A mixture was prepared by blending 8.4g of this resin with 1.2g of mercaptate ester Q43 and 0.4g of 2,2-dimethoxy-2-phenylacetophenone. A coating of the material was prepared as described in Example 2 and exposed to UV light from a Technocure 200 W/IN mercury lamp at an intensity of 50mW/cm? (365nm) for 30 secs. After this time, a dry to touch, soft, cured film was obtained. -14Example 8 To a solution of 122g 4-hydroxybenzaldehyde in 500 mis acetone was added 276g potassium carbonate. This mixture was stirred for 15 minutes. A solution of 133g allyl bromide in 200 mis acetone was then added dropwise over 30 minutes. The resulting mixture was heated at reflux for 1 hour, left standing for a further 16 hours and finally heated at reflux for 2 hours. After filtration, the solvent was removed by distillation leaving 175g of a reddish liquid. This residue was distilled under reduced pressure (B.Pt. 104°"114°C. at 1.5 mmHg) to yield 130g of a pale yellow liquid which was identified by infrared and n.m.r. spectroscopy as 4-allyloxybenzaldehyde.
To a solution of 9.36g potassium metal in 500 mis tert-butanol was added 85.68g methyl tri phenylphosphoniurn bromide. The resulting yellow suspension was stirred for 20 minutes and 32.4g 4-allyloxybenzaldehyde was then added over 10 minutes. This mixture was stirred for 30 minutes and then allowed to stand overnight. After filtration the solvent was removed under reduced pressure leaving 107g of a red semi-solid residue. Petroleum ether (B.Pt. 40°~60°C.) was added to the residue precipitating a solid which was filtered. After removal of the petroleum ether, the remaining resin was distilled under reduced pressure (B.Pt. 68°-82° C. at 0,4 mmHg) yielding 26.7g of a clear colorless liquid which was identified by infrared and n.m.r. spectroscopy as 4-allyloxystyrene (Proton IMMR: (CDCI3)δ =4.50, 4.58, doublet, allyloxymethylene protons; S =5.0-6.5, multiplets, allyl and vinyl group protons;8 =6.80, 6.95, 7.30 and 7.45, quartet, aromatic protons).
Example 9 UV sensitive compositions based on 4-allyloxystyrene (prepared as in Example 8) were formulated (quantities are all parts by weight): Composition E 4-allyloxystyrene Mercaptate ester, Q43 2,2!,-dimethoxy-2"phenyl acetophenonone 2 , 2-di ethoxyacetophenone 4-methyl-2s6-di-t-butylphenol 13,0 12.2 1.3 0.1 Composition F Composition G 13.0 8.0 12.2 12,2 1.3 1.3 0.1 0.1 -15A one mm thick coating of each of these compositions was prepared on a 1 x 4 microscope glass slide and exposed to UV light from a UVA LOC 1000W mercury lamp (Trade Mark Loctite Corp,) operating at 200W per inch. Compositions E and F gave a cured tack-free film after 30 secs, exposure. Composition G was cured tack-free after 10 secs, exposure. All of these coatings were insoluble in dichloromethane. Composition G gave a tougher coating than either E or F. In each case, the coating was located 14cms directly under the mercury arc. The light intensity at this point was measured using an Optical Associates Inc., light meter (model 206) with a 365nm probe and found to be 150mW/cm2.
Example 10 4-allyloxy-3-methoxystyrene was prepared from vanillin by a method analogous to that described in Example 8. In this case, the intermediate product 4-allyloxy-3-methoxybenzaldehyde was obtained by vacuum distillation at 152-158°C and 7mbar in 83% yield and the styryloxy derivative at 92-110QC and 0.5 mbar in 58% yield.
A UV sensitive composition was prepared by blending 9.5g 4-allyloxy-3methoxystyrene, 12.2g of mercaptate ester Q43, 0.9g 2,2-dimethoxy-2phenylacetophenone and 0.1g 4-methy1-2s6-di-i-butylphenol. A coating of the composition was prepared and irradiated as described in Example 9.
In this case, a tack-free, cured film was obtained after 15 secs.
Example 11 To a solution of 136g 4-hydroxyacetophenone in 500 mis acetone was added 276.41g potassium carbonate. This mixture was stirred for 15 minutes. A solution of 133g allyl bromide in 200 mis acetone was then added dropwise over 45 minutes, and the resulting mixture was stirred for a further 4 hours and left standing for a further 16 hours. Thin-layer chromatography showed some starting material to be present at the end of this time. The mixture was then heated to reflux for 4 hours and left standing a further 16 hours. After this time the solvent was removed by distillation leaving 230g of a brown liquid. This residue was distilled under reduced pressure (S.Pt. 107-115°C at 0.6mmHg.) to yield 158g of,pale yellow liquid which was identified by infrared and n.m.r. spectroscopy as 4-allyloxyacetophenone. -16To a solution-of 5.58g potassium metal in tert-butanol was added 51g methyl triphenylphosphonium bromide. The resulting yellow suspension was stirred for 20 minutes. A solution of 18.86g 4-allyloxyacetophenone in 30 mis tertbutanol was then added gradually and stirred for 16 hours at room temperature. After this time, the mixture was filtered and solvent removed under reduced pressure. The resulting mixture was extracted with petroleum ether to yield 28g of brown resin. This resin was distilled under reduced pressure (B.Pt. 88°C at 1mm Hg) yielding 15.21g of a clear colorless liquid which was identified by infrared and n.m.r. spectroscopy as 4-allyloxy isopropenyl benzene (Proton NMR: (CDC1,) 5= 2.12 singlet, «-methyl protons; 6= 4.50, 4.58, doublet, allyloxy methylene, protons; 5= 5.0-6.5, multiplets, allyl and vinyl group protons; δ= 6.80, 6.95, 7.35 and 7.50, quartet, aromatic protons).
A UV sensitive composition was prepared by blending 8.7g of this material, 12.2g of mercaptate ester Q43 and 0.8g 2,2-di:nethoxy-2-phenylacetophenone.
A 0.25mm thick coating was prepared and irradiated with UV light as described in Example 9. A tack-free cured film was obtained after 30 secs, exposure.
Example 12 4-allyloxy-3-methoxypropenylbenzene was prepared by refluxing a stirred mixture of isoeugenol (164g),allylbromide (133g) and potassium carbonate (278g) in dry acetone (700 mis) for 18 hours. Removal of the solids and solvent gave a crude product 208g which was vacuum distilled to yield 130g of pure 4-allyloxy-3-methoxy-prcn-l-enylbenzene (b.p. 104-118°C at 0.Imbar).
A UV sensitive composition was prepared by blending 10.3g of this material with 12.2 g of mercaptate ester Q43 and 0.9g 2,2-dimethoxy-2-phenylacetophenone A coating (0.25mm thick) was prepared and irradiated under UV light (as detailed in Example 9). A tack-free cured film was obtained after 10 secs, exposure.
Example 13 Isovanillin (76g) was dissolved in a stirred mixture of potassium carbonate (104g) and acetone (450mls) frllcwed by the dropwise addition of allyl bromide (67g) over ca. 20 mins. The mixture was refluxed for 5 hours, -17cooled and filtered. The solvent was removed from the filtrate under reduced pressure and the residue was distilled under vacuum to yield 3-allyloxy-4-methoxybenzaldehyde (85g), b.p. 137 - 150°C at 1.5mbar. 60MHz, ]HMR (CDC13) ?Ό.2 (ί , ΪΗ, CHO) , Z 2.45-3.1 (m, 3H, ArH) ,^3.6-4.9 (m, 3H, CH=CH2),t 5.35, (d, 2H, 0CH2),£6.1 (S, 3H, OCHj Sodium amide (39g) was dispersed in dry tetrahydrofuran (800mls). Methyltriphenylphosphonium bromide (102g) was added and the mixture stirred at R.T. for 2 hours. 3-al lyloxy-4-methoxy-benzaldehyde (50g) was then added dropwise over ca. 15mins. and the mixture stirred for a further 3 hours. The mixture was filtered and the solvent removed from the filtrate under reduced pressure. The residue was washed with diethyl ether (1.51) and the solvent removed to yield a brown coloured resin. The washing process was repeated and the residue obtained was distilled under reduced pressure to give 3-allyloxy-4methoxystyrene (29.5g), b.p,98-104°C at 0.8 mbar. 60MHz, ^HMR (CDC13)Or2.45-4.90 (m, 9H, ArH + vinyl CH=CH2 + allyl CH=CH2), t5.35 (d, 2H, 0CH2),776.1 (S, 3H, 0CH3).
A UV sensitive composition was prepared by blending 9.5g of this material with 12.2g of mercaptate ester Q43 and 0.9g 2,2-dimethoxy-2-phenylacetophenone 0.5mm thick coatings were prepared and irradiated with UV light as described in Example 9. After 10 secs, exposure, a tack-free cured film had formed.
Example 14 isoeugenol (16.46g), 1,4-dibromobutane (11.88g) and tetra-n-butylammonium bromide (3.22g) were added to a stirred suspension of potassium carbonate (20.7g) in dry toluene (lOOg). The mixture was heated at 105°C for 20 hrs. After this time t.l.c. analysis indicated that all of the starting isoeugenol had been consumed. The mixture was filtered and the toluene solution washed with water (3 x lOOmls), After drying (sodium sulphate), the toluene was removed under reduced pressure to yield 14.25g of a white solid. The solid was recrystal 1ised from a mixture of ethanol and chloroform to give 4.94g of a pure product of the structure: The m.p. was 135°C. The infra red spectrum showed no phenolic hydroxyl group, indicating that the pure dialkylated product had been isolated.
A UV sensitive composition was prepared by blending together a hot mixture of 1.9g of this material with 20.4g of 4-allyloxy-3-methoxy1-propenyl benzene as prepared in Example 12. On cooling, 25.4g of mercaptate ester Q43 and 0.23g of 2,2-diethoxyacetophenone were added. 0.25mm thick coatings of the composition were prepared and irradiated as detailed in Example 9. After 30 secs, exposure, a tack-free cured film was obtained.
Example 15 0-propenylphenol (67g) was added to a stirred suspension of potassium carbonate (138g) in dry acetone. Allyl bromide (67g) was then added dropwise over about 20 minutes and the stirred mixture was heated under reflux for 4 hours. After this time, gas liquid chromatography indicated that the phenol had been converted to about 95% of a mixture of cis and trans 2-allyloxy-1-propenylbenzene. The mixture was filtered and the solvent removed under reduced pressure. The residue was vacuum distilled and yielded 58.9g of almost pure 2-allyloxy-1-propenylbenzene which was identified spectroscopically. [b-P- 64-88°C at 0.6mbarJ. 60MHz, 'HMR (CDC13) : 2.6-5.0, 9H, muitiplets due to AR-H, -CH=CH? and -CH=CH- ; 5.5, doublet, 2H,0-CH?- ; 8.2, doublet 3H, -CH3 A UV sensitive composition was prepared by blending 8.7g of this styryloxy resin with 12.2g of mercaptate ester Q43 and 0.8g of 2,2-dimethoxy-2phenylacetophenone. A 0.25mm thick coating was prepared and irradiated as in Example 9. In this case, a tad I rec surface cure was obtained afte 10 seconds irradiation.
Claims (12)
1. Curable compositions comprising 1) a multifunctional styryloxy monomer having one or more of the following structures 5 wherei n R% R 2 and R 3 are selected from vinyl (-CH=CH2h 1propenyl ^CH=CH-CH3), isopropenyl (-C=CH2), hydrogen, ch 3 alkyl or alkoxy, provided that at least one of R^, R 2 and R 3 must be vinyl, l-propenyl or isopropenyl; 10 n is an integer £1; if n = 1, then R 4 is a monovalent hydrocarbon radical containing one free-radically copolymerisable alkenyl -20or cycloalkenyl group, if n£2, R 4 is a multivalent hydrocarbon radical which may contain a maximum of one free-radically copolymerisable alkenyl or eycloalkenyl group; r5 is a divalent hydrocarbon radical; or a carbon atom which is part of a cyclic group in the radical G; or a radical of formula ~R 7 -C-O- where R 7 is a divalent hydrocarbon radical; if n = 1, G is a monovalent organic or inorganic radical, free of phenolic hydroxyl groups or other groups which substantially interfere with radical polymerisation, containing one free-radically copolymerisable alkenyl or cycloalkenyl group; if n ^2, G is a multivalent organic or inorganic radical, free of phenolic hydroxyl groups or other groups which substantially interfere with radical polymerisation, which may contain a maximum of one free-radically copolymerisable alkenyl or cycloalkenyl group; R° is aC^-C^Q alkyl or cycloalkyl group; or if n = 1, R 6 may also be an alkenyl or cycloalkenyl group, provided that G does not contain an alkenyl or cycloalkenyl group.
2. ) a multifunctional thiol.
3. ) a free-radical curing rate accelerator. 2. A composition according to claim 1 wherein the mole ratio of styryloxy/thiol groups is from 0.2/1 to 5/1. -213. A composition according to claim 1 or 2 wherein the curing rate accelerator is present in an amount of 0.05-10% by weight of the total weight of the composition.
4. A composition according to any of claims 1 to 3 wherein R is an alkenyl group.
5. A composition according to claim 4 wherein R is an allylic group.
6.» A composition according to any of claims 1 to 5 wherein when n = 1, G is a substituted or unsubstituted straight or branched chain monovalent hydrocarbon radical which contains one free-radical ly copolymerisable alkenyl group.
7. A composition according to claim 6 wherein G is an allyl alkyl ether group, optionally substituted with a hydroxy group.
8. A composition according to claim 1 wherein the stryloxy monomer is selected from i) Reaction products of hydroxyl containing styryloxy compounds with a) Polyfunctional isocyanates b) Polyfunctional carboxylic acids or acid chlorides. c) Di anhydrides. d) Aldehydes. e) Polyepoxides. f) Polyfunctional esters. ii) Reaction products of 3-hydroxy-4-alkoxy styrenes with a) Polyfunctional isocyanates b) Di anhydrides c) Polyepoxides. d) Multifunctional acid chlorides.
9.-229. A composition according to any of claims 1 to 8 wherein the free radical curing rate accelerator is a photocuring rate accelerator
10. A method of providing a cured dry to the touch coating on a substrate comprising: 5 a) applying a composition as in claim 9 to the substrate surface, and b) irradiating the composition on the substrate for a time effective to cure the compound to a dry film.
11. A compound comprising the reaction product of a compound 10 of the formula: where R~ is vinyl, 1-propenyl or isopropenyl:, R 2 and R 3 are H, C^-C^ alkyl or alkoxy; and R 6 is alkyl, with an epoxy functional compound selected from: a) triglycidylether isocyanurate, b) allyl glycidyl ether, c) compounds having plural epoxy cyclohexane groups, and d) a multifunctional epoxidised polydimethyl siloxane which is the reaction product of allyl glycidyl ether with a di methyl siloxane having 2 or more SiH groups. „23
12. A Compound selected from:
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IE3286A IE60271B1 (en) | 1986-01-07 | 1986-01-07 | "Thiol/ene compositions" |
| DE8787300101T DE3784356T2 (en) | 1986-01-07 | 1987-01-07 | THIOL / ENE COMPOSITION. |
| EP87300101A EP0229033B1 (en) | 1986-01-07 | 1987-01-07 | Thiol/ene compositions |
| US07/351,310 US5021512A (en) | 1986-01-07 | 1989-05-04 | Thiol/ene compositions |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IE3286A IE60271B1 (en) | 1986-01-07 | 1986-01-07 | "Thiol/ene compositions" |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| IE60271L IE60271L (en) | 1987-07-07 |
| IE60271B1 true IE60271B1 (en) | 1994-06-29 |
Family
ID=11005633
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IE3286A IE60271B1 (en) | 1986-01-07 | 1986-01-07 | "Thiol/ene compositions" |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US5021512A (en) |
| EP (1) | EP0229033B1 (en) |
| DE (1) | DE3784356T2 (en) |
| IE (1) | IE60271B1 (en) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4640849A (en) * | 1986-01-31 | 1987-02-03 | Loctite (Ireland) Limited | Meta-bridged styryloxy resins |
| JPH0798851B2 (en) * | 1990-02-08 | 1995-10-25 | 信越化学工業株式会社 | Radiation curable composition |
| US5217760A (en) * | 1990-07-20 | 1993-06-08 | Loctite Corporation | Free radically curable formulations employing dithiolate catalysts |
| US5399624A (en) * | 1990-12-21 | 1995-03-21 | Loctite Corporation | High purity resins for thiol-ene polymerizations and method for producing same |
| US5208281A (en) * | 1991-02-05 | 1993-05-04 | Loctite Corporation | Stabilization of thiolene compositions |
| US5902838A (en) * | 1996-10-01 | 1999-05-11 | Loctite Corporation | Process for the assembly of glass devices subjected to high temperatures, compositions therefor and novel polymers for rheological control of such compositions |
| US6231714B1 (en) | 1998-11-24 | 2001-05-15 | Loctite Corporation | Allylic phenyl ether (meth)acrylate compositions and novel allylic phenyl ether (meth)acrylate monomers |
| US8044111B2 (en) * | 2007-11-30 | 2011-10-25 | Novartis Ag | Actinically-crosslinkable silicone-containing block copolymers |
| SG187632A1 (en) | 2010-07-30 | 2013-03-28 | Novartis Ag | Amphiphilic polysiloxane prepolymers and uses thereof |
| HUE044765T2 (en) | 2010-10-06 | 2019-11-28 | Novartis Ag | Polymerisable chain-extended polysiloxanes with pendant hydrophilic groups |
| CN108431172B (en) | 2015-12-31 | 2021-04-13 | 3M创新有限公司 | Article comprising particles with quantum dots |
| CN108473861A (en) | 2015-12-31 | 2018-08-31 | 3M创新有限公司 | Curable quantum dot composition and product |
| US20210238361A1 (en) * | 2020-01-30 | 2021-08-05 | Evonik Operations Gmbh | Process for producing high-purity hydrosilylation products |
| CN114516932B (en) * | 2020-11-19 | 2022-12-02 | 中国科学院福建物质结构研究所 | Bio-based transparent degradable flexible resin and preparation method thereof |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2488501A (en) * | 1948-09-13 | 1949-11-15 | Dow Chemical Co | 1, 4-di(alkenylphenoxy)-2-butenes |
| US3327019A (en) * | 1960-11-24 | 1967-06-20 | Bayer Ag | Diethers and copolymerizates therefrom |
| US3661744A (en) * | 1966-07-26 | 1972-05-09 | Grace W R & Co | Photocurable liquid polyene-polythiol polymer compositions |
| US3616041A (en) * | 1969-01-23 | 1971-10-26 | Grace W R & Co | Process for adhering two substrates with a liquid curable composition |
| US3663625A (en) * | 1970-04-23 | 1972-05-16 | Bechtel Int Corp | Bis(1-alkyl(or aryl)vinyl)p-phenylene oxide monomers |
| JPS5243514B2 (en) * | 1973-08-14 | 1977-10-31 | ||
| US4272586A (en) * | 1978-02-23 | 1981-06-09 | Denki Kagaku Kogyo Kabushiki Kaisha | Laminated glass product |
| DE2967466D1 (en) * | 1979-02-12 | 1985-07-18 | Gen Electric | Coating method and curable compositions |
| US4388450A (en) * | 1981-03-13 | 1983-06-14 | General Electric Company | Aromatic polyvinyl ethers and heat curable molding compositions obtained therefrom |
| US4486582A (en) * | 1983-01-27 | 1984-12-04 | The Dow Chemical Company | Reactive monomers and thermosettable compositions containing same |
| US4732956A (en) * | 1984-06-18 | 1988-03-22 | Loctite (Ireland) Ltd. | Styryloxy resins and compositions thereof |
| US4543397A (en) * | 1984-06-18 | 1985-09-24 | Loctite (Ireland) Ltd. | Styryloxy resins and compositions thereof |
| US4640849A (en) * | 1986-01-31 | 1987-02-03 | Loctite (Ireland) Limited | Meta-bridged styryloxy resins |
-
1986
- 1986-01-07 IE IE3286A patent/IE60271B1/en not_active IP Right Cessation
-
1987
- 1987-01-07 EP EP87300101A patent/EP0229033B1/en not_active Expired - Lifetime
- 1987-01-07 DE DE8787300101T patent/DE3784356T2/en not_active Expired - Fee Related
-
1989
- 1989-05-04 US US07/351,310 patent/US5021512A/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| US5021512A (en) | 1991-06-04 |
| EP0229033B1 (en) | 1993-03-03 |
| DE3784356D1 (en) | 1993-04-08 |
| IE60271L (en) | 1987-07-07 |
| EP0229033A2 (en) | 1987-07-15 |
| DE3784356T2 (en) | 1993-08-26 |
| EP0229033A3 (en) | 1988-10-12 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM4A | Patent lapsed |